Spontaneous Pulmonary Hypertension Associated With Systemic Sclerosis in P‐Selectin Glycoprotein Ligand 1–Deficient Mice

OBJECTIVE: Pulmonary arterial hypertension (PAH), one of the major complications of systemic sclerosis (SSc), is a rare disease with unknown etiopathogenesis and noncurative treatments. As mice deficient in P‐selectin glycoprotein ligand 1 (PSGL‐1) develop a spontaneous SSc‐like syndrome, we underto...

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Detalles Bibliográficos
Autores principales: González‐Tajuelo, Rafael, de la Fuente‐Fernández, María, Morales‐Cano, Daniel, Muñoz‐Callejas, Antonio, González‐Sánchez, Elena, Silván, Javier, Serrador, Juan Manuel, Cadenas, Susana, Barreira, Bianca, Espartero‐Santos, Marina, Gamallo, Carlos, Vicente‐Rabaneda, Esther F., Castañeda, Santos, Pérez‐Vizcaíno, Francisco, Cogolludo, Ángel, Jiménez‐Borreguero, Luis Jesús, Urzainqui, Ana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Systemic Sclerosis
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7065124/
https://www.ncbi.nlm.nih.gov/pubmed/31509349
http://dx.doi.org/10.1002/art.41100

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7065124/
https://www.ncbi.nlm.nih.gov/pubmed/31509349
http://dx.doi.org/10.1002/art.41100

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